Canonical Allele Identifier: CA1596380280

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149270_162149271delinsAC , CM000667.2:g.162149270_162149271delinsAC	GRCh38
NC_000005.9:g.161576276_161576277delinsAC , CM000667.1:g.161576276_161576277delinsAC	GRCh37
NC_000005.8:g.161508854_161508855delinsAC	NCBI36
NG_009290.1:g.86629_86630delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1086_1087delinsAC
ENST00000361925.9:c.1205_1206delinsAC	ENSP00000354651.5:p.Asn402=
ENST00000523372.2:c.1168_1169delinsAC
ENST00000638253.1:n.339_340delinsAC
ENST00000638552.1:c.800_801delinsAC	ENSP00000491763.1:p.Asn267=
ENST00000638660.1:c.800_801delinsAC	ENSP00000492869.1:p.Asn267=
ENST00000638772.1:c.1085_1086delinsAC	ENSP00000491557.1:p.Asn362=
ENST00000638877.1:c.962_963delinsAC
ENST00000639046.1:c.476_477delinsAC	ENSP00000492659.1:p.Asn159=
ENST00000639111.2:c.1085_1086delinsAC	ENSP00000492125.2:p.Asn362=
ENST00000639213.2:c.1085_1086delinsAC MANE Select	ENSP00000491909.2:p.Asn362=
ENST00000639278.1:c.1013_1014delinsAC	ENSP00000491958.1:p.Asn338=
ENST00000639384.1:c.1085_1086delinsAC	ENSP00000491240.1:p.Asn362=
ENST00000639424.1:c.*285_*286delinsAC	ENSP00000491245.1:n.*285_*286delinsAC
ENST00000639683.1:c.1019_1020delinsAC	ENSP00000492581.1:p.Asn340=
ENST00000639975.1:c.1019_1020delinsAC	ENSP00000492096.1:p.Asn340=
ENST00000640500.1:n.383_384delinsAC
ENST00000640574.1:c.800_801delinsAC	ENSP00000491582.1:p.Asn267=
ENST00000640739.1:n.3616_3617delinsAC
ENST00000640910.1:c.523_524delinsAC
ENST00000640985.1:c.998_999delinsAC	ENSP00000492293.1:p.Asn333=
ENST00000641017.1:c.1085_1086delinsAC	ENSP00000493461.1:p.Asn362=
ENST00000356592.7:c.1085_1086delinsAC	ENSP00000349000.3:p.Asn362=
ENST00000361925.8:c.1085_1086delinsAC	ENSP00000354651.4:p.Asn362=
ENST00000414552.6:c.1205_1206delinsAC	ENSP00000410732.2:p.Asn402=
ENST00000522990.5:c.*687_*688delinsAC	ENSP00000430732.1:n.*687_*688delinsAC
ENST00000523372.1:c.1206_1207delinsAC	ENSP00000430124.1:n.1206_1207delinsAC
NM_000816.3:c.1085_1086delinsAC	NP_000807.2:p.Asn362=
NM_198903.2:c.1205_1206delinsAC	NP_944493.2:p.Asn402=
NM_198904.2:c.1085_1086delinsAC	NP_944494.1:p.Asn362=
NM_001375339.1:c.1076_1077delinsAC	NP_001362268.1:p.Asn359=
NM_001375340.1:c.923-2460_923-2459delinsAC	NP_001362269.1:n.923-2460_923-2459delinsAC
NM_001375341.1:c.1082_1083delinsAC	NP_001362270.1:p.Asn361=
NM_001375342.1:c.1082_1083delinsAC	NP_001362271.1:p.Asn361=
NM_001375343.1:c.1205_1206delinsAC	NP_001362272.1:p.Asn402=
NM_001375344.1:c.1124_1125delinsAC	NP_001362273.1:p.Asn375=
NM_001375345.1:c.1019_1020delinsAC	NP_001362274.1:p.Asn340=
NM_001375346.1:c.1019_1020delinsAC	NP_001362275.1:p.Asn340=
NM_001375347.1:c.998_999delinsAC	NP_001362276.1:p.Asn333=
NM_001375348.1:c.665_666delinsAC	NP_001362277.1:p.Asn222=
NM_001375349.1:c.800_801delinsAC	NP_001362278.1:p.Asn267=
NM_001375350.1:c.665_666delinsAC	NP_001362279.1:p.Asn222=
NM_198904.3:c.1085_1086delinsAC	NP_944494.1:p.Asn362=
NM_198904.4:c.1085_1086delinsAC MANE Select	NP_944494.1:p.Asn362=